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从人类粪便标本中直接扩增和基因分型脆弱双核阿米巴。

Direct amplification and genotyping of Dientamoeba fragilis from human stool specimens.

作者信息

Peek Ron, Reedeker Freek R, van Gool Tom

机构信息

Department of Medical Microbiology, Tropical Medicine and AIDS, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

J Clin Microbiol. 2004 Feb;42(2):631-5. doi: 10.1128/JCM.42.2.631-635.2004.

Abstract

Dientamoeba fragilis is a globally occurring parasite that has been recognized as a causative agent of gastrointestinal symptoms. A single-round PCR was developed to detect D. fragilis DNA directly from human stool samples. The genetic diversity of D. fragilis from 93 patients and 6 asymptomatic carriers was examined by PCR followed by restriction fragment length polymorphism and sequencing of part of the small-subunit rRNA gene. The data show that D. fragilis sequences can be studied directly from fecal specimens despite the absence of a cyst stage and without the need for prior culturing. In addition, the results suggest strongly that D. fragilis shows remarkably little variation in its small-subunit rRNA gene.

摘要

脆弱双核阿米巴是一种在全球范围内存在的寄生虫,已被确认为胃肠道症状的病原体。开发了一种单轮聚合酶链反应(PCR),用于直接从人类粪便样本中检测脆弱双核阿米巴的DNA。通过PCR检测93例患者和6名无症状携带者的脆弱双核阿米巴的遗传多样性,随后进行限制性片段长度多态性分析,并对小亚基核糖体RNA基因的部分序列进行测序。数据表明,尽管没有包囊阶段且无需预先培养,但仍可直接从粪便标本中研究脆弱双核阿米巴序列。此外,结果强烈表明,脆弱双核阿米巴的小亚基核糖体RNA基因变异极小。

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